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Analytical "bake-off" of whole genome sequencing quality for the Genome Russia project using a small cohort for autoimmune hepatitis. [electronic resource] by
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- Tamazian, Gaik
- Rotkevich, Mikhail
- Krasheninnikova, Ksenia
- Evsyukov, Igor
- Sidorov, Sviatoslav
- Dobrynin, Pavel
- Yurchenko, Andrey A
- Shimansky, Valentin
- Shcherbakova, Irina V
- Glotov, Andrey S
- Valle, David L
- Tang, Minzhong
- Shin, Emilia
- Schwarz, Kathleen B
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Producer: 20190117
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PloS one vol. 13
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Biological significance of the defense mechanisms against oxidative damage in nucleic acids caused by reactive oxygen species: from mitochondria to nuclei. [electronic resource] by
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- Ide, Yasuhito
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- Tominaga, Yohei
- Furuichi, Masato
- Sakumi, Kunihiko
Producer: 20040617
In:
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Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia. [electronic resource] by
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- Lane, Jessica
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- Chan, Sandy
- Huang, Alden
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- Perlman, Susan
- Geschwind, Daniel H
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Producer: 20120711
In:
Movement disorders : official journal of the Movement Disorder Society vol. 27
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EGFR-activating mutations correlate with a Fanconi anemia-like cellular phenotype that includes PARP inhibitor sensitivity. [electronic resource] by
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- Greninger, Patricia
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- Willers, Henning
Producer: 20140506
In:
Cancer research vol. 73
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PrimPol bypasses UV photoproducts during eukaryotic chromosomal DNA replication. [electronic resource] by
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Molecular cell vol. 52
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Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes. [electronic resource] by
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- Davoine, Claire-Sophie
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- Ewenczyk, Claire
- Ding, Jinhui
- Gibbs, J Raphael
- Hannequin, Didier
- Melki, Judith
- Toutain, Annick
- Laugel, Vincent
- Forlani, Sylvie
- Charles, Perrine
- Broussolle, Emmanuel
- Thobois, Stéphane
- Afenjar, Alexandra
- Anheim, Mathieu
- Calvas, Patrick
- Castelnovo, Giovanni
- de Broucker, Thomas
- Vidailhet, Marie
- Moulignier, Antoine
- Ghnassia, Robert T
- Tallaksen, Chantal
- Mignot, Cyril
- Goizet, Cyril
- Le Ber, Isabelle
- Ollagnon-Roman, Elisabeth
- Pouget, Jean
- Brice, Alexis
- Singleton, Andrew
- Durr, Alexandra
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In:
JAMA neurology vol. 75
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Microprocessor, Setx, Xrn2, and Rrp6 co-operate to induce premature termination of transcription by RNAPII. [electronic resource] by
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- Contreras, Xavier
- Harwig, Alex
- Laurent-Chabalier, Sabine
- Nakamura, Mirai
- Chen, Xin
- Zhang, Ke
- Meziane, Oussama
- Boyer, Frédéric
- Parrinello, Hugues
- Berkhout, Ben
- Terzian, Christophe
- Benkirane, Monsef
- Kiernan, Rosemary
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In:
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PrimPol, an archaic primase/polymerase operating in human cells. [electronic resource] by
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- Mourón, Silvana
- Terrados, Gloria
- Powell, Christopher
- Salido, Eduardo
- Méndez, Juan
- Holt, Ian J
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Molecular cell vol. 52
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A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia. [electronic resource] by
- Al Tassan, Nada
- Khalil, Dania
- Shinwari, Jameela
- Al Sharif, Latifa
- Bavi, Prashant
- Abduljaleel, Zainularifeen
- Abu Dhaim, Nada
- Magrashi, Amna
- Bobis, Steve
- Ahmed, Hala
- Alahmed, Samaher
- Bohlega, Saeed
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In:
Human mutation vol. 33
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Down-regulation of MTHFD2 inhibits NSCLC progression by suppressing cycle-related genes. [electronic resource] by
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- Yang, Lehe
- Cai, Mengsi
- Zhou, Feng
- Xiao, Sisi
- Li, Yaozhe
- Wan, Tingting
- Cheng, Dezhi
- Wang, Liangxing
- Zhao, Chengguang
- Huang, Xiaoying
Producer: 20210423
In:
Journal of cellular and molecular medicine vol. 24
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